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IL59345A0 - Silicone-containing bis-ether and bis-thioether aromatic amines and their manufacture - Google Patents

Silicone-containing bis-ether and bis-thioether aromatic amines and their manufacture

Info

Publication number
IL59345A0
IL59345A0 IL59345A IL5934580A IL59345A0 IL 59345 A0 IL59345 A0 IL 59345A0 IL 59345 A IL59345 A IL 59345A IL 5934580 A IL5934580 A IL 5934580A IL 59345 A0 IL59345 A0 IL 59345A0
Authority
IL
Israel
Prior art keywords
group
chem
bis
functional
different
Prior art date
Application number
IL59345A
Original Assignee
M & T Chemicals Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by M & T Chemicals Inc filed Critical M & T Chemicals Inc
Publication of IL59345A0 publication Critical patent/IL59345A0/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
    • H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
    • H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
    • H01B3/46—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes silicones
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/0834—Compounds having one or more O-Si linkage
    • C07F7/0838—Compounds with one or more Si-O-Si sequences
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804—Compounds having Si-O-C linkages
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/4007—Curing agents not provided for by the groups C08G59/42 - C08G59/66
    • C08G59/4085—Curing agents not provided for by the groups C08G59/42 - C08G59/66 silicon containing compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/38—Polysiloxanes modified by chemical after-treatment

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Silicon Polymers (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)

Abstract

Novel silicones having the general formula <CHEM> wherein Q is an aromatic nucleus, Z is -S- @-, <CHEM> or -O-, R is a bivalent group or a functional bivalent group, each R<1> is chosen from monovalent hydrocarbon radicals and functional hydrocarbon radicals and any one R<1> may be the same as or different from another R<1>, R<3> is hydrogen or a hydrocarbon radical or a functional group or atom, x is O or an integer of 1 or more, F is a functional group or atom, with the proviso that F is not primary amino when Z is other than -O-, and T is a group chosen from alkoxy, aryloxy or other substituted or unsubstituted oxyhydrocarbyl radical and a group having the general formula <CHEM> wherein Q, Z, R, R<1>, R<3> and F are as defined above and any one R may be the same as or different from the other R and one R @ may be different from the other R<3>. These compounds may be made by reacting the compound <CHEM> where G denotes alkoxy or aryloxy or other substituted or unsubstituted oxyhydrocarbyl radical under conditions set out in the specification. The compounds are suitable for making copolymers of silcones with other organic chemicals, curing catalysts for epoxies, urethane and the like.
IL59345A 1979-02-13 1980-02-08 Silicone-containing bis-ether and bis-thioether aromatic amines and their manufacture IL59345A0 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US1190179A 1979-02-13 1979-02-13

Publications (1)

Publication Number Publication Date
IL59345A0 true IL59345A0 (en) 1980-05-30

Family

ID=21752444

Family Applications (1)

Application Number Title Priority Date Filing Date
IL59345A IL59345A0 (en) 1979-02-13 1980-02-08 Silicone-containing bis-ether and bis-thioether aromatic amines and their manufacture

Country Status (7)

Country Link
EP (1) EP0014599B1 (en)
JP (1) JPS55129293A (en)
KR (1) KR840001782B1 (en)
AT (1) ATE20237T1 (en)
CA (1) CA1185613A (en)
DE (1) DE3071626D1 (en)
IL (1) IL59345A0 (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES491385A0 (en) * 1979-08-08 1981-05-16 A METHOD FOR PREPARING A SILANO
US4511701A (en) * 1984-02-27 1985-04-16 General Electric Company Heat curable epoxy resin compositions and epoxy resin curing agents
DE3935638A1 (en) * 1989-10-26 1991-05-02 Consortium Elektrochem Ind ORGANOSILYL ALKYL FLAVORS
US5300669A (en) * 1991-11-28 1994-04-05 Dow Corning Toray Silicone Co., Ltd. Methylphenethyl functional silicones
KR100480666B1 (en) * 2001-08-14 2005-04-06 한국화학연구원 Silicon compound having functional groups and method of improving the surface of an inorganic solid using same
FR2830188B1 (en) 2001-09-28 2005-01-28 Oreal TINCTORIAL COMPOSITION CONTAINING A PARA-AMINOPHENOL OR PARA-PHENYLENE DIAMINE COMPOUND SUBSTITUTED WITH A SILANIC RADICAL
US8119710B2 (en) 2005-09-21 2012-02-21 Basf Se Filled rubber compounds with improved processability
CN110229182A (en) * 2019-07-03 2019-09-13 北京航空航天大学 A kind of organo-silicon coupling agent and preparation method thereof

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1054041A (en) * 1900-01-01
US2783262A (en) * 1954-11-22 1957-02-26 Dow Corning Halophenoxysiloxanes
US2863898A (en) * 1957-07-05 1958-12-09 Dow Corning Pentachlorobenzenethiolmethyl substituted organosiloxanes
GB1062418A (en) * 1964-01-27 1967-03-22 Ici Ltd New nitrogen-containing siloxanes
DE2215629A1 (en) * 1972-03-30 1973-10-04 Dynamit Nobel Ag CORE SUBSTITUTED ARALKYL SILANES
FR2245663A1 (en) * 1973-08-17 1975-04-25 Rhone Progil Aminophenoxy alkyl silanes and dimers, polymers - by catalytic hydrogenation of corresponding nitrophenols
FR2286832A1 (en) * 1974-10-01 1976-04-30 Rhone Poulenc Ind SILICA ETHYLENIC COMPOUNDS WITH FUNCTIONAL GROUPS
US4139547A (en) * 1978-05-17 1979-02-13 Bergston & Associates, Inc. Silicone containing bis-thioether aromatic amines

Also Published As

Publication number Publication date
EP0014599A2 (en) 1980-08-20
ATE20237T1 (en) 1986-06-15
DE3071626D1 (en) 1986-07-10
EP0014599A3 (en) 1981-07-01
CA1185613A (en) 1985-04-16
JPS55129293A (en) 1980-10-06
EP0014599B1 (en) 1986-06-04
KR830001962A (en) 1983-05-21
KR840001782B1 (en) 1984-10-20

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